On the public citation graph

Norlignans, Acylphloroglucinols, and a Dimeric Xanthone from Hypericum chinense

https://doi.org/10.1021/np1004483
0 signed · 76 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1099-1573(200003)14:2<139::aid-ptr608>3.0.co;2-8openalex-snapshot
The effect of reserpine, a modulator of multidrug efflux pumps, on the in vitro activity of tetracycline against clinical isolates of methicillin resistant Staphylococcus aureus (MRSA) possessing the tet(K) determinant
inferredcites →https://doi.org/10.1002/mrc.1270091106openalex-snapshot
Carbon‐13 n.m.r. study of naturally occurring xanthones
inferredcites →https://doi.org/10.1016/0031-9422(94)00862-nopenalex-snapshot
Spiro-lactones, hyperolactone A-D from Hypericum chinense
inferredcites →https://doi.org/10.1016/0195-6701(93)90007-mopenalex-snapshot
Characterization of a strain of methicillin-resistant Staphylococcus aureus (EMRSA-15) by conventional and molecular methods
inferredcites →https://doi.org/10.1016/0195-6701(95)90191-4openalex-snapshot
A major outbreak of methicillin-resistant Staphylococcus aureus caused by a new phage-type (EMRSA-16)
inferredcites →https://doi.org/10.1016/j.bpc.2004.10.001openalex-snapshot
NMR spectroscopic, mass spectroscopic, X-ray crystallographic, and theoretical studies of molecular mechanics of natural products: farformolide B and sesamin
inferredcites →https://doi.org/10.1016/j.phytochem.2006.05.043openalex-snapshot
Xanthones from Hypericum chinense
inferredcites →https://doi.org/10.1016/s0367-326x(02)00082-5openalex-snapshot
The genus Hypericum—a valuable resource of anti-Staphylococcal leads
inferredcites →https://doi.org/10.1021/np0704147openalex-snapshot
Polyisoprenylated Benzoylphloroglucinol Derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1021/np900109yopenalex-snapshot
Acylphloroglucinol, Biyouyanagiol, Biyouyanagin B, and Related Spiro-lactones from Hypericum chinense
inferredcites →https://doi.org/10.1021/np9702953openalex-snapshot
(+)-Episesaminone, a Sesamum indicum Furofuran Lignan. Isolation and Hemisynthesis
inferredcites →https://doi.org/10.1021/ol050960wopenalex-snapshot
Biyouyanagin A, an Anti-HIV Agent from Hypericum chinense L. var. salicifolium
inferredcites →https://doi.org/10.1093/jac/24.6.851openalex-snapshot
Characterisation and molecular cloning of the novel macrolide-streptogramin B resistance determinant from Staphylococcus epidermidis
inferredcites →https://doi.org/10.1097/00000441-200508000-00007openalex-snapshot
Clinical Characteristics of Linezolid-Resistant Staphylococcus aureus Infections
inferredcites →https://doi.org/10.1128/aac.37.5.1086openalex-snapshot
Efflux-mediated fluoroquinolone resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1246/cl.1987.1337openalex-snapshot
Antimicrobial Compounds, Chinesin I and II from Flowers of Hypericum chinense L.
inferredcites →https://doi.org/10.1246/cl.1989.683openalex-snapshot
Novel Spiro-Compound, Hyperolactone from Hypericum chinense L.
inferredcites →https://doi.org/10.1248/cpb.55.19openalex-snapshot
Xanthones from Stems of Hypericum chinense

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112970zenodo-depositor-declared
Chemical constituents from the flowers of Hypericum monogynum L. with COX-2 inhibitory activity
inferred← citeshttps://doi.org/10.1002/adsc.202000762openalex-snapshot
Recent Advancements on Transition‐Metal‐Catalyzed, Chelation‐Induced ortho‐Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/ajoc.201300086openalex-snapshot
Total Synthesis of ent‐Hyperione A and ent‐Hyperione B
inferred← citeshttps://doi.org/10.1002/ajoc.202000635openalex-snapshot
Copper‐Catalyzed Tandem Cross‐Coupling/Annulation of Phenols with Ketoximes through Dual C−H Functionalization: Synthesis of Substituted 2‐Aryl‐1H‐indoles
inferred← citeshttps://doi.org/10.1002/ange.201103227openalex-snapshot
Enantioselektive enzymatische Desymmetrisierung prochiraler Allendiole
inferred← citeshttps://doi.org/10.1002/ange.201207479openalex-snapshot
Synthesis of ortho‐Acylphenols through the Palladium‐Catalyzed Ketone‐Directed Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/anie.201103227openalex-snapshot
Enantioselective Enzymatic Desymmetrization of Prochiral Allenic Diols
inferred← citeshttps://doi.org/10.1002/anie.201207479openalex-snapshot
Synthesis of ortho ‐Acylphenols through the Palladium‐Catalyzed Ketone‐Directed Hydroxylation of Arenes
inferred← citeshttps://doi.org/10.1002/cbdv.201100433openalex-snapshot
New Lignans and Their Biological Activities
inferred← citeshttps://doi.org/10.1002/cbdv.202100944openalex-snapshot
Isolation and Identification of Acylphloroglucinols in the Medicinal Plant,Melaleuca alternifolia(Australian Tea Tree)
inferred← citeshttps://doi.org/10.1007/978-3-319-14185-5_1openalex-snapshot
Butanones: Monoketones
inferred← citeshttps://doi.org/10.1007/s10600-015-1429-yopenalex-snapshot
Two New Flavones from Hypericum chinense and Their Anti-Tobacco Mosaic Virus Activity
inferred← citeshttps://doi.org/10.1016/b978-0-12-800874-4.00023-4openalex-snapshot
Antimicrobial Secondary Metabolites—Extraction, Isolation, Identification, and Bioassay
inferred← citeshttps://doi.org/10.1016/b978-0-323-85542-6.00013-5openalex-snapshot
Medicinal plants in antimicrobial resistance—Perspectives towards drug development
inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00006-0openalex-snapshot
Progress in the Syntheses of Dibenzocyclooctadiene Lignans
inferred← citeshttps://doi.org/10.1016/bs.armc.2020.06.001openalex-snapshot
Antimicrobial natural products
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.07.023openalex-snapshot
Natural product derived promising anti-MRSA drug leads: A review
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.08.035openalex-snapshot
Total syntheses of hyperaspidinols A and B enabled by a bioinspired diastereoselective cascade sequence
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.08.010openalex-snapshot
Acylphloroglucinols from the leaves of Callistemon viminalis
inferred← citeshttps://doi.org/10.1016/j.foodres.2015.02.023openalex-snapshot
Aboriginal bush foods: A major phloroglucinol from Crimson Bottlebrush flowers (Callistemon citrinus, Myrtaceae) displays strong antinociceptive and anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112669openalex-snapshot
Callistemon citrinus bioactive metabolites as new inhibitors of methicillin-resistant Staphylococcus aureus biofilm formation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114798openalex-snapshot
Glycosidic phenylpropanoid dimers and trimers from Castanopsis choboensis and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.03.008openalex-snapshot
Tectonoelins, new norlignans from a bioactive extract of Tectona grandis
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104247openalex-snapshot
Chemical constituents from Hypericum japonicum and their PXR agonistic activity
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.008openalex-snapshot
Pd-catalyzed oxidative acylation of 2-phenoxypyridines with alcohols via C–H bond activation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.009openalex-snapshot
Palladium catalyzed addition of arylboronic acid or indole to nitriles: synthesis of aryl ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.08.044openalex-snapshot
N-Acylsuccinimides: Efficient acylative coupling reagents in palladium-catalyzed Suzuki coupling via C N cleavage
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.09.062openalex-snapshot
One-pot synthesis of ortho -acylphenols by palladium-catalyzed phenol C–H addition to nitriles
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00878openalex-snapshot
Anti-inflammatory Dimeric Tetrahydroxanthones from an Endophytic Muyocopron laterale
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00066openalex-snapshot
Hypermongones A–J, Rare Methylated Polycyclic Polyprenylated Acylphloroglucinols from the Flowers of Hypericum monogynum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00224openalex-snapshot
Synthesis of Natural Acylphloroglucinol-Based Antifungal Compounds against Cryptococcus Species
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00525openalex-snapshot
Anti-Staphylococcal Calopins from Fruiting Bodies of Caloboletus radicans
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02697openalex-snapshot
Palladium-Catalyzed Denitrogenative Synthesis of Aryl Ketones from Arylhydrazines and Nitriles Using O2 as Sole Oxidant
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01744openalex-snapshot
One-Pot Synthesis of Furo[3,4-c]indolo[2,1-a]isoquinolines through Rh(III)-Catalyzed Cascade Reactions of 2-Phenylindoles with 4-Hydroxy-2-alkynoates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01970openalex-snapshot
Concise Construction of the Tricyclic Core of Bullataketals Enabled by a Biomimetic Intermolecular (3 + 3) Type Cycloaddition
inferred← citeshttps://doi.org/10.1021/ol300153fopenalex-snapshot
Nickel-Catalyzed Intermolecular Insertion of Aryl Iodides to Nitriles: A Novel Method to Synthesize Arylketones
inferred← citeshttps://doi.org/10.1039/c2ob27073kopenalex-snapshot
Chemoenzymatic total synthesis of hyperiones A and B
inferred← citeshttps://doi.org/10.1039/c4np00050aopenalex-snapshot
Xanthone dimers: a compound family which is both common and privileged
inferred← citeshttps://doi.org/10.1039/c9cc02170aopenalex-snapshot
An unexpected multi-component one-pot cascade reaction to access furanobenzodihydropyran-fused polycyclic heterocycles
inferred← citeshttps://doi.org/10.1039/d0ob00077aopenalex-snapshot
“On water” palladium catalyzed diastereoselective boronic acid addition to structurally diverse cyclopropane nitriles
inferred← citeshttps://doi.org/10.1039/d0sc05556eopenalex-snapshot
Cu-catalyzed hydroxycyclopropanol ring-opening cyclization to tetrahydrofurans and tetrahydropyrans: short total syntheses of hyperiones
inferred← citeshttps://doi.org/10.1039/d1nj05170aopenalex-snapshot
Design, synthesis and evaluation of structurally diverse ortho -acylphenol-diindolylmethane hybrids as anticancer agents
inferred← citeshttps://doi.org/10.1039/d2ob00288dopenalex-snapshot
Metal-catalyzed reactions of organic nitriles and boronic acids to access diverse functionality
inferred← citeshttps://doi.org/10.1039/d5qo01477hopenalex-snapshot
Recent advances in the total synthesis of polycyclic phloroglucinol natural products
inferred← citeshttps://doi.org/10.1177/1934578x1400900223openalex-snapshot
Methicillin-resistant Staphylococcus aureus , Vancomycin-resistant Enterococcus faecalis and Enterococcus faecium active Dimeric Isobutyrylphloroglucinol from Ivesia gordonii
inferred← citeshttps://doi.org/10.1371/journal.pone.0028737openalex-snapshot
Ellagic Acid Derivatives from Rubus ulmifolius Inhibit Staphylococcus aureus Biofilm Formation and Improve Response to Antibiotics
inferred← citeshttps://doi.org/10.2174/1389557518666181017143141openalex-snapshot
Antimicrobial Effects of Chemical Compounds Isolated from Traditional Chinese Herbal Medicine (TCHM) Against Drug-Resistant Bacteria: A Review Paper
inferred← citeshttps://doi.org/10.3389/fmicb.2022.952633openalex-snapshot
Breaking down the cell wall: Still an attractive antibacterial strategy
inferred← citeshttps://doi.org/10.3389/fphar.2020.555715openalex-snapshot
Inhibitory Effects of Twenty-Nine Compounds From Potentilla longifolia on Lipid Accumulation and Their Mechanisms in 3T3-L1 Cells
inferred← citeshttps://doi.org/10.3390/molecules23081865openalex-snapshot
A Short and Efficient Total Synthesis of Ficuseptamines A and B
inferred← citeshttps://doi.org/10.3390/molecules24020220openalex-snapshot
9-Norlignans: Occurrence, Properties and Their Semisynthetic Preparation from Hydroxymatairesinol
inferred← citeshttps://doi.org/10.3390/molecules25010197openalex-snapshot
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review
inferred← citeshttps://doi.org/10.3390/molecules25214976openalex-snapshot
Gold(I)-Catalyzed Domino Reaction for Furopyrans Synthesis
inferred← citeshttps://doi.org/10.3390/molecules30040967openalex-snapshot
Xanthone Dimers in Angiosperms, Fungi, Lichens: Comprehensive Review of Their Sources, Structures, and Pharmacological Properties
inferred← citeshttps://doi.org/10.3390/v10070360openalex-snapshot
Anti-Infectivity against Herpes Simplex Virus and Selected Microbes and Anti-Inflammatory Activities of Compounds Isolated from Eucalyptus globulus Labill.
inferred← citeshttps://doi.org/10.3762/bjoc.11.29openalex-snapshot
Synthesis of the furo[2,3-b]chromene ring system of hyperaspindols A and B
inferred← citeshttps://doi.org/10.3987/com-13-12842openalex-snapshot
Cytotoxic Xanthones from Hypericum chinense
inferred← citeshttps://doi.org/10.3987/rev-14-sr(k)1openalex-snapshot
Prenylated Acylphloroglucinols and Meroterpenoids from Hypericum Plants
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.